A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464138



Internal ID21121691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28219454..28227596hg38UCSC Ensembl
chr12:28372387..28380529hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg388143
hg198143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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